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assistant manager / manager quality assurance Jobs in Karachi

assistant manager – financial reporting (night) Jobs in Karachi

assistant manager – treasury & payables (night shift) Jobs in Karachi

assistant/manager-quality & regulatory compliance Jobs in Karachi

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billing executive (fresh) (night shift)

quality assurance associate clinical trial data evening shift

Minerva Research Solutions

<div>JOB DESCRIPTION: 
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Our services include Data Operations, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
Responsibilities:<ul><li>
Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.</li><li>
Ensure data is recorded in accordance with sponsor protocol, GCP guidelines, industry guidelines and agency regulations.</li><li>
Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.</li><li>
Provide ongoing compliance support including but not limited to:</li><li>
Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.</li><li>
Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).</li><li>
Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.</li><li>
Assist in preparing for all Sponsor and FDA audits.</li><li>
Assist in conducting internal audits to review key processes.</li><li>
Provides appropriate support to assigned cross-functional workgroups.</li><li>
Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.</li><li>
Query resolution, data entry, and questionnaire preparation regarding the respective studies.</li><li>
Other related Quality Assurance projects as assigned.</li><li>
The QA Associate will report to the Quality Assurance Lead</li></ul>
Knowledge, Education, and Experience:<ul><li>
Fresh MBBS with keen interest in Clinical Research are strongly encouraged to apply, PharmD graduates will also be prefered.</li><li>
In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.</li><li>
Knowledge of IRB requirements.</li><li>
1+ years in work related to Quality Control / Quality Assurance area in clinical research.</li><li>
Experience including external clinical/regulatory and document auditing will be a plus</li></ul>
Skills and Abilities:<ul><li>
Good communication skills (interpersonal, written, verbal)</li><li>
Strong attention to detail and good time management skills</li><li>
Flexible attitude with respect to work assignments</li><li>
Ability to manage multiple and varied tasks in a fast-moving environment</li><li>
Ability to interact professionally at all levels within the organization.</li><li>
Knowledge of HIPAA Privacy Act and its application to clinical research.</li></ul>
Benefits:<ul><li>
Competitive salary and performance-based bonuses.</li><li>
Medical health insurance coverage.</li><li>
Employees Old-age benefits coverage.</li><li>
Flexible work hours and remote work options.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul>
Openings:
03 positions (Evening shift) 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
xaiHnpkG7W</div>

Quality Assurance Associate (Clinical Trial Data)(Evening Shift)

<div>
 
 JOB DESCRIPTION:
 
 
 
 Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
 
 
 Our services include Data Operations, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.
 
 
 We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
 
 
 Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
 
 
 
 Responsibilities:
 
 
 
 <ul>
 <li>
 Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness
 </li>
 <li>
 Ensure data is recorded in accordance with sponsor protocol, GCP guidelines, industry guidelines and agency regulations
 </li>
 <li>
 Perform quality control checks; identify and track source documentation errors and non-conformances with requirements
 </li>
 <li>
 Provide ongoing compliance support including but not limited to:
 </li>
 <li>
 Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans
 </li>
 <li>
 Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs)
 </li>
 <li>
 Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities
 </li>
 <li>
 Assist in preparing for all Sponsor and FDA audits
 </li>
 <li>
 Assist in conducting internal audits to review key processes
 </li>
 <li>
 Provides appropriate support to assigned cross-functional workgroups
 </li>
 <li>
 Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement
 </li>
 <li>
 Query resolution, data entry, and questionnaire preparation regarding the respective studies
 </li>
 <li>
 Other related Quality Assurance projects as assigned
 </li>
 <li>
 The QA Associate will report to the Quality Assurance Lead
 
 
 </li>
 </ul>
 
 Knowledge, Education, and Experience:
 
 
 
 <ul>
 <li>
 Fresh MBBS with keen interest in Clinical Research are strongly encouraged to apply, PharmD graduates will also be prefered
 </li>
 <li>
 In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials
 </li>
 <li>
 Knowledge of IRB requirements
 </li>
 <li>
 1+ years in work related to Quality Control / Quality Assurance area in clinical research
 </li>
 <li>
 Experience including external clinical/regulatory and document auditing will be a plus
 
 
 </li>
 </ul>
 
 Skills and Abilities:
 
 
 
 <ul>
 <li>
 Good communication skills (interpersonal, written, verbal)
 </li>
 <li>
 Strong attention to detail and good time management skills
 </li>
 <li>
 Flexible attitude with respect to work assignments
 </li>
 <li>
 Ability to manage multiple and varied tasks in a fast-moving environment
 </li>
 <li>
 Ability to interact professionally at all levels within the organization
 </li>
 <li>
 Knowledge of HIPAA Privacy Act and its application to clinical research
 
 
 </li>
 </ul>
 
 Benefits:
 
 
 
 <ul>
 <li>
 Competitive salary and performance-based bonuses
 </li>
 <li>
 Medical health insurance coverage
 </li>
 <li>
 Employees Old-age benefits coverage
 </li>
 <li>
 Flexible work hours and remote work options
 </li>
 <li>
 Professional learning and development support
 </li>
 <li>
 Generous vacation and paid time off
 </li>
 <li>
 Employee assistance programs for mental health
 </li>
 <li>
 Company-sponsored events and team-building activities
 </li>
 <li>
 Diverse, professional and inclusive work environment
 </li>
 <li>
 Opportunities for career growth
 </li>
 <li>
 Cutting-edge technology and tools
 </li>
 <li>
 Family-friendly policies, including parental leave
 </li>
 <li>
 Commuter benefits or transportation assistance
 </li>
 <li>
 Social responsibility and community involvement programs
 
 
 </li>
 </ul>
 
 Openings:
 
 
 
 03 positions
 
 (Evening shift)
 
 
 
 Full-time
 
 
 On-site job
 
 
 
 Work Schedule Timings:
 
 
 
 Monday to Friday
 
 
 7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 
 
 Powered by JazzHR
 
 
 xaiHnpkG7W
</div>

LN Technologies

ob description:LN Technologies, a subsidiary of App Maisters Inc USA, is an Enterprise App Development company that specializes in developing Mobility, Web, BI, and Cloud-based solutions. With over 400 successful projects under our portfolio, we take pride in catering to the needs of all sizes and types of clients, from ambitious startups &amp; small businesses to large multinationals.We are seeking a motivated and detail-oriented BioMedical Research Scientist to support innovation in the biomedical and biosciences domains. This role involves identifying strategic collaboration opportunities, conducting in-depth market and scientific research, and supporting grant and research paper writing efforts. You will work closely with cross-functional teams and stakeholders to drive innovation aligned with emerging trends and funding landscapes.Key Responsibilities:<ul><li>Conduct comprehensive research on individuals, businesses, universities, and non-profits to assess eligibility, expertise, and strategic fit for collaboration.</li><li>Analyze funding history, research expertise, and past participation using public records, proprietary databases, and research tools.</li><li>Identify and develop research-driven ideas aligned with current biomedical and bioscience trends and funding opportunities.</li><li>Monitor and interpret key developments in biomedical innovation, public health initiatives, and emerging technologies.</li><li>Conduct market research and gather market intelligence to identify competitive positioning, white space, and industry needs.</li><li>Prepare reports and presentations summarizing key insights and strategic recommendations.</li><li>Assist in writing and editing research papers, white papers, and grant applications.</li><li>Perform comprehensive literature reviews and synthesize information from peer-reviewed journals, government databases, and clinical trials.</li><li>Collect, interpret, and analyze data from diverse sources such as PubMed, NIH RePORTER, clinical trial registries, and scientific publications.</li><li>Support data visualization and presentation for internal and external stakeholders.</li></ul>Required Qualifications:<ul><li>Currently pursuing a PhD in Biomedical Engineering &amp; Biomedical Technology / Sciences</li><li>Experience:</li><li>Minimum +1 year of research experience in a biomedical or biosciences domain.</li><li>Demonstrated experience in research writing, including literature reviews or academic papers.</li><li>Familiarity with academic research methodologies, ethics, and compliance.</li></ul>Job Type: Full-timeApplication Question(s):<ul><li>Are you comfortable working on the Evening Shift?</li><li>What is your Current Salary?</li><li>What is your expected salary?</li><li>How soon can you join?</li><li>Are you currently enrolled in a PhD program in Biomedical Engineering &amp; Biomedical Technology / Sciences or a related field?</li></ul>Work Location: In person

Biomedical Researcher - Evening Shift

<div>Location: Karachi 
 Department: Patient Experience &amp; Support 
 Employment Type: Full-Time | Night Shift<h2 class="jobSectionHeader">
Who We Are</h2>
Minerva Research Solutions is a leading Clinical Trial Management and Support organization, dedicated to elevating global healthcare outcomes through innovation, operational excellence, and uncompromising quality.
We partner with biotech, pharmaceutical, and healthcare institutions to deliver integrated services across the clinical trial value chain, from feasibility to closeout.
Our portfolio spans Data Operations, Patient Recruitment, and Regulatory Services, enabling clients to accelerate the development of breakthrough therapies with accuracy, agility, and regulatory confidence.
Governed by globally recognized standards such as FDA regulations and ICH-GCP, we ensure data integrity, participant safety, and reliable insights at every stage.
We are expanding our Customer Experience function and seeking a Spanish-speaking, customer-centric professional to join our high-performance team.<h1 class="jobSectionHeader">
Role Summary</h1>
As a Spanish Call Center Representative, you will be the frontline ambassador for Minerva, providing support to Spanish-speaking patients, partners, and stakeholders. You will ensure accurate, empathetic, and compliant communication, representing our values and service standards.<h1 class="jobSectionHeader">
Key Responsibilities</h1><ul><li>
Manage inbound and outbound interactions for Spanish-speaking patients and clients with professionalism and accuracy.</li><li>
Deliver a frictionless customer journey, proactively resolving concerns and providing tailored support.</li><li>
Support appointments, participant onboarding, and study-related communication while ensuring confidentiality.</li><li>
Maintain all interactions according to clinical research regulations and service quality standards.</li><li>
Collaborate with cross-functional teams to ensure timely issue resolution.</li><li>
Keep accurate CRM documentation for all interactions.</li><li>
Identify service gaps and escalate complex cases appropriately.</li><li>
Uphold Minerva&rsquo;s CX standards at all touchpoints.</li></ul><h1 class="jobSectionHeader">
Required Qualifications &amp; Experience</h1><ul><li>
Bachelor&rsquo;s degree in any discipline (or equivalent).</li><li>
Fluent in Spanish and English (neutral/US accent preferred in English).</li><li>
Minimum 1 year of international customer support experience (BPO, contact center, or shared services).</li><li>
Experience in healthcare, life sciences, or clinical research is a plus.</li><li>
Strong analytical thinking, emotional intelligence, and client-service orientation.</li><li>
Comfortable in a target-driven, high-volume, fast-paced environment.</li><li>
Proficient with CRM tools and MS Office applications.</li><li>
Willingness to work night shifts and adapt to business needs.</li></ul><h1 class="jobSectionHeader">
What You&rsquo;ll Gain at Minerva</h1><ul><li>
Competitive salary with performance-based incentives</li><li>
Comprehensive medical insurance &amp; EOBI benefits</li><li>
Structured Learning &amp; Development programs and certifications</li><li>
Paid leave: annual, medical, casual</li><li>
Mental well-being and employee support programs</li><li>
Inclusive, collaborative, and growth-oriented culture</li><li>
Internal recognition &amp; engagement initiatives</li><li>
Technology-forward workplace</li><li>
Transportation facility for female staff &amp; conveyance allowance for male staff</li><li>
Night shift allowance</li><li>
Family-supportive policies, including parental leave</li><li>
Opportunities to contribute to community and social impact initiatives</li></ul><h1 class="jobSectionHeader">
Work Schedule</h1>
Monday &ndash; Friday 
 7:00 PM &ndash; 3:00 AM (On-site)<h1 class="jobSectionHeader">
Diversity, Equity &amp; Inclusion</h1>
Minerva Research Solutions is an Equal Opportunity Employer. We value diverse perspectives, encourage innovation, and empower every individual to reach their full potential.
0YEkxLxJQC</div>

Spanish-Speaking Call Center Representative (Night Shift – Onsite)

SuperGame

Job Title: Community Media Host (Female) Location: Supergame Indoor Sports &amp; Gaming Center, Bahadurabad, Karachi Type: Full-time (On-site) Shift: Evening &amp; Night (peak hours)Role SummaryWe are hiring a confident and friendly female individual to interact with visitors and capture daily activity inside Supergame for social media. This is an on-floor role &mdash; you will be present among customers, not working remotely.Responsibilities<ul><li>Welcome and engage with customers</li><li>Help first-time visitors feel comfortable</li><li>Record daily photos/videos of games and player moments (with permission)</li><li>Capture busy hours, reactions and group activities</li><li>Assist in creating Instagram stories and reels</li><li>Encourage customers to follow and tag Supergame</li><li>Cover events, tournaments and busy nights</li><li>Coordinate content with the social media manager</li></ul>Requirements<ul><li>Comfortable talking to new people</li><li>Friendly, energetic personality</li><li>Regular Instagram user</li><li>Basic mobile video recording and editing skills</li><li>Punctual and reliable</li><li>Comfortable working evening/late hours</li></ul>Note: This is not a receptionist or work-from-home editing job. Work happens inside the venue.Selection: Shortlisted applicants will be invited for a brief on-site trial to create sample content.Job Type: Full-timePay: Up to Rs75,000.00 per monthWork Location: In person

Community Media Host (Female)

Mamji Hospital

Position: Resident Medical Officer (RMO) &ndash; Paeds ER (Evening Shift)Location: Karachi Department: Pediatric Emergency Room (Paeds ER) Shift: Evening ShiftJob Description:<ul><li>Provide immediate medical care and assessment to pediatric patients in the Emergency Room.</li><li>Evaluate, diagnose, and manage emergency and acute pediatric cases.</li><li>Monitor patient condition, vital signs, and treatment response.</li><li>Assist consultants in pediatric emergency procedures and critical care.</li><li>Maintain accurate medical records and ensure proper documentation.</li><li>Coordinate with nursing staff and relevant departments for patient care and admissions.</li><li>Ensure adherence to hospital policies and pediatric emergency care protocols.</li></ul>Requirements:<ul><li>Qualification: MBBS with valid registration from Pakistan Medical and Dental Council (PMDC/PMC). FCPS training in Pediatrics completed or in progress will be preferred.</li><li>Experience: Minimum 1&ndash;2 years of relevant experience in Pediatric Emergency Room.</li><li>Skills:</li><li>Strong pediatric clinical assessment skills</li><li>Ability to handle pediatric emergency cases efficiently</li><li>Good communication and teamwork skills</li><li>Ability to work effectively in evening shifts</li></ul>Job Type: Full-timeWork Location: In person

Resident Medical Officer (RMO) – Paeds ER (Evening Shift)

Position: Resident Medical Officer (RMO) &ndash; Adult ER (Evening Shift)Location: Karachi Department: Emergency Room (Adult ER) Shift: EveningJob Description:<ul><li>Provide immediate medical care and assessment to patients presenting in the Adult Emergency Room.</li><li>Perform initial evaluation, diagnosis, and management of emergency cases.</li><li>Monitor patient condition, vital signs, and response to treatment.</li><li>Assist consultants and senior doctors in emergency procedures and critical care management.</li><li>Maintain accurate and timely patient medical records and documentation.</li><li>Ensure compliance with hospital policies, protocols, and emergency care standards.</li><li>Coordinate with nursing staff and other departments for patient management and transfer.</li><li>Respond promptly to emergency situations and provide life-saving interventions when required.</li></ul>Requirements:<ul><li>Qualification: MBBS with valid registration from Pakistan Medical and Dental Council (PMDC/PMC). FCPS training completed or in progress will be preferred.</li><li>Experience: Minimum 2 years of relevant experience in Adult Emergency Room.</li><li>Skills:</li><li>Strong clinical assessment and decision-making skills</li><li>Ability to handle emergency and critical care patients</li><li>Good communication and teamwork abilities</li><li>Ability to work efficiently in night shifts and high-pressure environments</li></ul>Job Type: Full-timeWork Location: In person

RMO Adult ER (Evening)

Explore 1183+ Quality assurance associate clinical trial data evening shift in Karachi this March. Find roles across top companies and apply now to boost your career.

1183 quality assurance associate clinical trial data evening shift jobs In Karachi

Quality Assurance Associate (Clinical Trial Data)(Evening Shift)

Quality Assurance Associate (Clinical Trial Data)(Evening Shift)

Biomedical Researcher - Evening Shift

Spanish-Speaking Call Center Representative (Night Shift – Onsite)

Community Media Host (Female)

Resident Medical Officer (RMO) – Paeds ER (Evening Shift)

RMO Adult ER (Evening)